Torrent Joan, Lange Reinhard, Rezaei Human
From the Institut National de la Recherche Agronomique, UR892, Virologie Immunologie Moléculaires, Domaine de Vilvert, F-78350 Jouy-en-Josas, France and
the Institut National de la Recherche Agronomique, UMR1208, Ingénierie des Agropolymères et Technologies Emergentes, Université Montpellier, F-34095 Montpellier, France.
J Biol Chem. 2015 Aug 14;290(33):20417-26. doi: 10.1074/jbc.M115.661710. Epub 2015 Jun 30.
Protein oligomerization has been associated with a wide range of diseases. High pressure approaches offer a powerful tool for deciphering the underlying molecular mechanisms by revealing volume changes associated with the misfolding and assembly reactions. We applied high pressure to induce conformational changes in three distinct β-sheet-rich oligomers of the prion protein PrP, a protein characterized by a variety of infectious quaternary structures that can propagate stably and faithfully and cause diseases with specific phenotypic traits. We show that pressure induces dissociation of the oligomers and leads to a lower volume monomeric PrP state that refolds into the native conformation after pressure release. By measuring the different pressure and temperature sensitivity of the tested PrP oligomers, we demonstrate significantly different void volumes in their quaternary structure. In addition, by focusing on the kinetic and energetic behavior of the pressure-induced dissociation of one specific PrP oligomer, we reveal a large negative activation volume and an increase in both apparent activation enthalpy and entropy. This suggests a transition state ensemble that is less structured and significantly more hydrated than the oligomeric state. Finally, we found that site-specific fluorescent labeling allows monitoring of the transient population of a kinetic intermediate in the dissociation reaction. Our results indicate that defects in atomic packing may deserve consideration as a new factor that influences differences between PrP assemblies and that could be relevant also for explaining the origin of prion strains.
蛋白质寡聚化与多种疾病相关。高压方法为揭示与错误折叠和组装反应相关的体积变化从而破译潜在分子机制提供了一个强大工具。我们对朊病毒蛋白PrP的三种不同的富含β折叠的寡聚体施加高压以诱导构象变化,PrP是一种具有多种可稳定且忠实地传播并导致具有特定表型特征疾病的感染性四级结构的蛋白质。我们发现压力诱导寡聚体解离并导致体积更小的单体PrP状态,该状态在压力释放后重新折叠成天然构象。通过测量所测试的PrP寡聚体的不同压力和温度敏感性,我们证明其四级结构中的空穴体积存在显著差异。此外,通过关注一种特定PrP寡聚体压力诱导解离的动力学和能量行为,我们揭示了一个大的负活化体积以及表观活化焓和熵的增加。这表明过渡态系综的结构比寡聚态更少且水合程度显著更高。最后,我们发现位点特异性荧光标记能够监测解离反应中动力学中间体的瞬态群体。我们的结果表明原子堆积缺陷可能值得作为影响PrP组装体之间差异的一个新因素来考虑,并且这也可能与解释朊病毒株的起源相关。